Canonical Allele Identifier: PA658674959
Gene: WFS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 452350
ClinVar RCV Id: RCV000519714 RCV002509078
ClinVar Variation Id: 1966944
ClinVar RCV Id: RCV002721671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005996.2:p.Phe374Leu
CA356174298
NM_006005.3:c.1120T>C
CA356174303
NM_006005.3:c.1122C>A
CA356174304
NM_006005.3:c.1122C>G